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Gene : CLDN9 Homo sapiens

Name  ? claudin 9 Cytological Location  16p13.3
Brief Description  claudin 9
Description  This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. This protein is one of the entry cofactors for hepatitis C virus. Mouse studies revealed that this gene is required for the preservation of sensory cells in the hearing organ and the gene deficiency is associated with deafness. [provided by RefSeq, Jun 2010]
  • synonyms:
  • CLDN9,
  • OTTHUMG00000129000,
  • AJ130941,
  • NM_020982,
  • uc010uwo.1,
  • HGNC:2051
  • identifiers:
  • 9080,
  • ENSG00000213937,
  • CLDN9

Genome feature

Region: gene ? Length: 1583  
Location: 16:3012923-3014505 Cyto location: 16p13.3


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Function

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Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Interactions

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Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

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Other

3753 SN Ps

4 Cross References

14 Data Sets

15 Homologues

0 Located Features

97 Rna Seq Results